1.
Chem Commun (Camb)
; 51(68): 13283-5, 2015 Sep 04.
Artículo
en Inglés
| MEDLINE
| ID: mdl-26197760
RESUMEN
Mannosylations with benzylidene protected mannosyl donors were found to be ß-selective even when no preactivation was performed. It was also found that the kinetic ß-product in some cases anomerizes fast to the thermodynamically favored α-anomer under typical reaction conditions.